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Regulation No. 26 of 2012 of Minister of Social Affairs of Estonia on Procedure for providing safety information about medicinal products, for calculating the fees charged for the safety and quality monitoring of medicinal products and for the payment of such fees

Country
Estonia
Type of law
Regulation
Date of original text
Source
FAO , FAOLEX
Abstract
This regulation establishes the procedure for providing safety information about medicinal products, for calculating the fees charged for the safety and quality monitoring of medicinal products and for the payment of such fees. The physician, dentist, veterinarian, nurse, midwife or user of a medicinal product informs the State Agency of Medicines of an adverse reaction to a medicinal product, using the electronic form of the adverse reaction report or a paper report.
Attached files
http://faolex.fao.org/docs/pdf/est196376.pdf
http://faolex.fao.org/docs/pdf/est196376EST.pdf
Web site
http://www.riigiteataja.ee
Date of consolidation/reprint
Repealed
No
Serial Imprint
RT I, 18.07.2012, 7
Source language

English

Legislation Amendment
No
Original title
Eesti sotsiaalministri 2012. aasta m rus nr 26 Ravimi ohutusalase teabe edastamise ning ravimi ohutus- ja kvaliteediseire tasu arvestamise ja tasumise kord
Implements
Medicinal Products Act.
Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products.
Directive 2004/28/EC of the European Parliament and of the Council amending Directive 2001/82/EC on the Community code relating to veterinary medicinal products.
Commission Directive 2009/9/EC amending Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to medicinal products for veterinary use.